Strain identifier

BacDive ID: 5057

Type strain: No

Species: Proteus mirabilis

Strain history: CIP <- 1994, ATCC <- FDA: strain PCI 765

NCBI tax ID(s): 584 (species)

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General

@ref: 446

BacDive-ID: 5057

DSM-Number: 788

keywords: 16S sequence, Bacteria, aerobe, Gram-negative, motile, rod-shaped, human pathogen

description: Proteus mirabilis DSM 788 is an aerobe, Gram-negative, motile human pathogen of the family Morganellaceae.

NCBI tax id

  • NCBI tax id: 584
  • Matching level: species

strain history

@refhistory
446<- ATCC <- FDA, strain PCI 765
120969CIP <- 1994, ATCC <- FDA: strain PCI 765

doi: 10.13145/bacdive5057.20240510.9

Name and taxonomic classification

LPSN

  • @ref: 20215
  • description: domain/bacteria
  • keyword: phylum/pseudomonadota
  • domain: Bacteria
  • phylum: Pseudomonadota
  • class: Gammaproteobacteria
  • order: Enterobacterales
  • family: Morganellaceae
  • genus: Proteus
  • species: Proteus mirabilis
  • full scientific name: Proteus mirabilis Hauser 1885 (Approved Lists 1980)

@ref: 446

domain: Bacteria

phylum: Proteobacteria

class: Gammaproteobacteria

order: Enterobacteriales, not validated

family: Morganellaceae

genus: Proteus

species: Proteus mirabilis

full scientific name: Proteus mirabilis Hauser 1885

type strain: no

Morphology

cell morphology

  • @ref: 120969
  • gram stain: negative
  • cell shape: rod-shaped
  • motility: yes

Culture and growth conditions

culture medium

@refnamegrowthlinkcomposition
446NUTRIENT AGAR (DSMZ Medium 1)yeshttps://mediadive.dsmz.de/medium/1Name: NUTRIENT AGAR (DSMZ Medium 1) Composition: Agar 15.0 g/l Peptone 5.0 g/l Meat extract 3.0 g/l Distilled water
35612MEDIUM 3 - Columbia agaryesColumbia agar (39.000 g);distilled water (1000.000 ml)
446COLUMBIA BLOOD MEDIUM (DSMZ Medium 693)yeshttps://mediadive.dsmz.de/medium/693Name: COLUMBIA BLOOD MEDIUM (DSMZ Medium 693) Composition: Defibrinated sheep blood 50.0 g/l Columbia agar base
120969CIP Medium 3yeshttps://catalogue-crbip.pasteur.fr/fiche_milieu.xhtml?crbip=3

culture temp

@refgrowthtypetemperature
446positivegrowth37
35612positivegrowth30
50915positivegrowth37
120969positivegrowth10-41
120969nogrowth5

Physiology and metabolism

oxygen tolerance

@refoxygen tolerance
50915aerobe
120969facultative anaerobe

metabolite utilization

@refmetaboliteutilization activitykind of utilization testedChebi-ID
68371Potassium 5-ketogluconate+builds acid from
68371Potassium 2-ketogluconate+builds acid from
68371gluconate+builds acid from24265
68371L-arabitol-builds acid from18403
68371D-arabitol-builds acid from18333
68371L-fucose-builds acid from18287
68371D-fucose-builds acid from28847
68371D-tagatose-builds acid from16443
68371D-lyxose-builds acid from62318
68371turanose-builds acid from32528
68371gentiobiose-builds acid from28066
68371xylitol-builds acid from17151
68371glycogen-builds acid from28087
68371starch-builds acid from28017
68371raffinose-builds acid from16634
68371melezitose-builds acid from6731
68371inulin-builds acid from15443
68371trehalose+builds acid from27082
68371sucrose+builds acid from17992
68371melibiose-builds acid from28053
68371lactose-builds acid from17716
68371maltose-builds acid from17306
68371cellobiose-builds acid from17057
68371salicin-builds acid from17814
68371esculin-builds acid from4853
68371arbutin-builds acid from18305
68371amygdalin-builds acid from27613
68371N-acetylglucosamine+builds acid from59640
68371methyl alpha-D-glucopyranoside-builds acid from320061
68371methyl alpha-D-mannoside-builds acid from43943
68371D-sorbitol-builds acid from17924
68371D-mannitol-builds acid from16899
68371myo-inositol-builds acid from17268
68371galactitol-builds acid from16813
68371L-rhamnose-builds acid from62345
68371L-sorbose-builds acid from17266
68371D-mannose+builds acid from16024
68371D-fructose+builds acid from15824
68371D-glucose+builds acid from17634
68371D-galactose+builds acid from12936
68371methyl beta-D-xylopyranoside-builds acid from74863
68371ribitol-builds acid from15963
68371L-xylose-builds acid from65328
68371D-xylose+builds acid from65327
68371D-ribose+builds acid from16988
68371L-arabinose-builds acid from30849
68371D-arabinose+builds acid from17108
68371erythritol-builds acid from17113
68371glycerol+builds acid from17754
68368L-arabinose-fermentation30849
68368amygdalin-fermentation27613
68368melibiose-fermentation28053
68368sucrose-fermentation17992
68368L-rhamnose-fermentation62345
68368sorbitol-fermentation30911
68368myo-inositol-fermentation17268
68368D-mannitol-fermentation16899
68368D-glucose+fermentation17634
68368gelatin-hydrolysis5291
68368tryptophan-energy source27897
68368urea+hydrolysis16199
68368citrate+assimilation16947
68368ornithine+degradation18257
68368lysine-degradation25094
68368arginine-hydrolysis29016
120969citrate+carbon source16947
120969glucose+fermentation17234
120969lactose-fermentation17716
120969nitrate+reduction17632
120969nitrite-reduction16301
120969malonate-assimilation15792
120969sodium thiosulfate+builds gas from132112
120969glucose+degradation17234
68374ornithine+degradation18257
68374arginine-hydrolysis29016
68374lysine-degradation25094
68374urea+hydrolysis16199
68374L-arabitol-builds acid from18403
68374D-galacturonic acid-builds acid from18024
68374Potassium 5-ketogluconate-builds acid from
68374D-mannitol-builds acid from16899
68374maltose-builds acid from17306
68374ribitol-builds acid from15963
68374palatinose-builds acid from18394
68374malonate-assimilation15792
68374tryptophan-energy source27897
68374D-glucose-builds acid from17634
68374sucrose-builds acid from17992
68374L-arabinose-builds acid from30849
68374D-arabitol-builds acid from18333
68374trehalose+builds acid from27082
68374L-rhamnose-builds acid from62345
68374myo-inositol-builds acid from17268
68374cellobiose-builds acid from17057
68374sorbitol-builds acid from30911

antibiotic resistance

  • @ref: 120969
  • metabolite: 0129 (2,4-Diamino-6,7-di-iso-propylpteridine phosphate)
  • is antibiotic: yes
  • is sensitive: no
  • is resistant: yes

metabolite production

@refChebi-IDmetaboliteproduction
6837435581indoleno
6836835581indoleno
6836816136hydrogen sulfideno
12096935581indoleno

metabolite tests

@refChebi-IDmetaboliteindole testvoges-proskauer-testmethylred-test
6837435581indole-
6836835581indole-
12096915688acetoin-
12096917234glucose+

enzymes

@refvalueactivityec
68374L-aspartate arylamidase+3.4.11.21
68374alpha-maltosidase-
68374alpha-galactosidase-3.2.1.22
68374alpha-glucosidase-3.2.1.20
68374beta-galactosidase-3.2.1.23
68374N-acetyl-beta-glucosaminidase-3.2.1.52
68374beta-glucuronidase-3.2.1.31
68374beta-glucosidase-3.2.1.21
68374lipase-
68374urease+3.5.1.5
68374lysine decarboxylase-4.1.1.18
68374arginine dihydrolase-3.5.3.6
68374ornithine decarboxylase+4.1.1.17
68368cytochrome oxidase-1.9.3.1
68368gelatinase-
68368tryptophan deaminase+4.1.99.1
68368urease+3.5.1.5
68368ornithine decarboxylase+4.1.1.17
68368lysine decarboxylase-4.1.1.18
68368arginine dihydrolase-3.5.3.6
68368beta-galactosidase-3.2.1.23
120969oxidase-
120969beta-galactosidase-3.2.1.23
120969alcohol dehydrogenase-1.1.1.1
120969gelatinase-
120969catalase+1.11.1.6
120969lysine decarboxylase-4.1.1.18
120969ornithine decarboxylase+4.1.1.17
120969tryptophan deaminase+
120969urease+3.5.1.5

API 20E

@refONPGADH ArgLDC LysODCCITH2SURETDA TrpINDVPGELGLUMANINOSorRHASACMELAMYARAOX
446---++-++---+---------
446---++-++-+-+---------

API 50CHac

@refGLYERYDARALARARIBDXYLLXYLADOMDXGALGLUFRUMNESBERHADULINOMANSORMDMMDGNAGAMYARBESCSALCELMALLACMELSACTREINUMLZRAFAMDGLYGXLTGENTURLYXTAGDFUCLFUCDARLLARLGNT2KG5KG
120969+-+-++---++++--------+--------++--------------+++

API ID32E

@refODCADH ArgLDC LysURELARLGAT5KGLIPRPbeta GLUMANMALADOPLEbeta GURMNTINDbeta NAGbeta GALGLUSACLARADARLalpha GLUalpha GALTRERHAINOCELSORalphaMALAspA
50915+--+---------------------+-----+

Safety information

risk assessment

@refpathogenicity humanpathogenicity animalbiosafety levelbiosafety level comment
446yesyes2Risk group (German classification)
1209692Risk group (French classification)

Sequence information

16S sequences

  • @ref: 20218
  • description: Proteus mirabilis strain ATCC 14153 16S ribosomal RNA gene, partial sequence
  • accession: FJ971887
  • length: 797
  • database: nuccore
  • NCBI tax ID: 584

External links

@ref: 446

culture collection no.: DSM 788, ATCC 14153, IMET 11232, CCUG 32232, PCI 765, CIP 104032

straininfo link

  • @ref: 74552
  • straininfo: 92372

literature

topicPubmed-IDtitleauthorsjournalDOIyearmeshtopic2
Pathogenicity8728063An abietane diterpene and two phenolics from Salvia forskahlei.Ulubelen A, Sonmez U, Topcu G, Bozok Johansson CPhytochemistry10.1016/0031-9422(95)00888-81996Anti-Bacterial Agents, Anti-Infective Agents/*chemistry/isolation & purification/pharmacology, Bacillus subtilis/drug effects, Bacteria/*drug effects, Candida albicans/drug effects, Diterpenes/*chemistry/isolation & purification/pharmacology, Enterococcus faecalis/drug effects, Escherichia coli/drug effects, Klebsiella pneumoniae/drug effects, Microbial Sensitivity Tests, Phenols/*chemistry/isolation & purification/pharmacology, Plant Roots, *Plants, Medicinal, Proteus mirabilis/drug effects, Pseudomonas aeruginosa/drug effects, Staphylococcus aureus/drug effects, Staphylococcus epidermidis/drug effects, Streptococcus agalactiae/drug effectsEnzymology
Pathogenicity12666252Synthesis and antimicrobial activity of [2-[2-(N, N-disubstituted thiocarbamoyl-sulfanyl)-acylamino] thiazol-4-yl]acetic acid ethyl esters.Ates O, Gursoy A, Altintas H, Otuk G, Birteksoz SArch Pharm (Weinheim)10.1002/ardp.2003900022003Anti-Bacterial Agents/*chemical synthesis/chemistry/pharmacology, Antitubercular Agents/*chemical synthesis/chemistry/pharmacology, Microbial Sensitivity Tests, Mycobacterium tuberculosis/*drug effects, Structure-Activity Relationship, Thiazoles/*chemical synthesis/chemistry/pharmacology
Pathogenicity15038463Synthesis of some new 6-methylimidazo[2,1-b]thiazole-5-carbohydrazide derivatives and their antimicrobial activities.Ur F, Cesur N, Birteksoz S, Otuk GArzneimittelforschung10.1055/s-0031-12969472004Anti-Infective Agents/*chemical synthesis/*pharmacology, Bacteria/drug effects, Chemical Phenomena, Chemistry, Physical, Fungi/drug effects, Hydrazines/*chemical synthesis/*pharmacology, Indicators and Reagents, Magnetic Resonance Spectroscopy, Microbial Sensitivity Tests, Spectrometry, Mass, Electrospray Ionization, Spectrophotometry, Ultraviolet, Spectroscopy, Fourier Transform Infrared, Thiazoles/*chemical synthesis/*pharmacology
Pathogenicity16129517Synthesis and antimicrobial activity of some novel derivatives of benzofuran: part 1. Synthesis and antimicrobial activity of (benzofuran-2-yl)(3-phenyl-3-methylcyclobutyl) ketoxime derivatives.Koca M, Servi S, Kirilmis C, Ahmedzade M, Kazaz C, Ozbek B, Otuk GEur J Med Chem10.1016/j.ejmech.2005.07.0042005Anti-Infective Agents/*chemical synthesis/chemistry/*pharmacology, Bacteria/drug effects, Benzofurans/*chemical synthesis/chemistry/*pharmacology, Microbial Sensitivity Tests, Molecular Structure, Oximes/*chemical synthesis/chemistry/*pharmacology, Structure-Activity Relationship
Pathogenicity16618017Synthesis and evaluation of antimicrobial and anticonvulsant activities of some new 3-[2- (5-aryl-1,3,4-oxadiazol-2-yl/4-carbethoxymethylthiazol-2-yl) imino-4-thiazolidinon-5-ylidene]-5-substituted/nonsubstituted 1H-indole-2-ones and investigation of their structure-activity relationships.Altintas H, Ates O, Uyde-Dogan BS, Alp FI, Kaleli D, Ozdemir O, Birteksoz S, Otuk G, Atana D, Uzun MArzneimittelforschung2006Anti-Infective Agents/*chemical synthesis/*pharmacology, Anticonvulsants/*chemical synthesis/*pharmacology, Antifungal Agents/chemical synthesis/pharmacology, Bacteria/drug effects, Fungi/drug effects, Gas Chromatography-Mass Spectrometry, Indicators and Reagents, Indoles/*chemical synthesis/*pharmacology, Magnetic Resonance Spectroscopy, Microbial Sensitivity Tests, Pentylenetetrazole/antagonists & inhibitors, Seizures/chemically induced/prevention & control, Spectrometry, Mass, Electrospray Ionization, Spectrophotometry, Infrared, Spectrophotometry, Ultraviolet, Structure-Activity Relationship, Thiazoles/*chemical synthesis/*pharmacology
Pathogenicity21877950Phenolic compounds and biological activity of Kitaibelia vitifolia.Maskovic P, Solujic S, Mihailovic V, Mladenovic M, Cvijovic M, Mladenovic J, Acamovic-Dokovic G, Kurcubic VJ Med Food10.1089/jmf.2011.00132011Anti-Bacterial Agents/*pharmacology, Antifungal Agents/*pharmacology, Aspergillus niger, Bacillus subtilis/drug effects, Candida albicans/drug effects, Escherichia coli/drug effects, Flavonoids/pharmacology, Free Radical Scavengers/*pharmacology, Gallic Acid/pharmacology, Klebsiella pneumoniae/drug effects, Lipid Peroxidation/drug effects, Malvaceae/*chemistry, Microbial Sensitivity Tests, Phenols/*pharmacology, Plant Extracts/*pharmacology, Proteus mirabilis/drug effects, Proteus vulgaris/drug effects, Staphylococcus aureus/drug effects
Pathogenicity23037005Impact of pH on activity of trimethoprim, fosfomycin, amikacin, colistin and ertapenem in human urine.Burian A, Erdogan Z, Jandrisits C, Zeitlinger MPharmacology10.1159/0003424232012Amikacin/pharmacology, Anti-Bacterial Agents/*pharmacology, Bacteria/*drug effects, Colistin/pharmacology, Ertapenem, Fosfomycin/pharmacology, Humans, Hydrogen-Ion Concentration, Microbial Sensitivity Tests, Trimethoprim/pharmacology, Urine/*chemistry, beta-Lactams/pharmacology

Reference

@idauthorscataloguedoi/urltitlejournalpubmed
446Curators of the DSMZLeibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSM 788)https://www.dsmz.de/collection/catalogue/details/culture/DSM-788
20215Parte, A.C., Sardà Carbasse, J., Meier-Kolthoff, J.P., Reimer, L.C. and Göker, M.10.1099/ijsem.0.004332List of Prokaryotic names with Standing in Nomenclature (LPSN) moves to the DSMZ
20218Verslyppe, B., De Smet, W., De Baets, B., De Vos, P., Dawyndt P.10.1016/j.syapm.2013.11.002StrainInfo introduces electronic passports for microorganisms.Syst Appl Microbiol. 37: 42-50 201424321274
35612Curators of the CIPhttps://brclims.pasteur.fr/brcWeb/souche/detail/1/15895
50915Curators of the CCUGCulture Collection University of Gothenburg (CCUG) (CCUG 32232)https://www.ccug.se/strain?id=32232
68368Automatically annotated from API 20E
68371Automatically annotated from API 50CH acid
68374Automatically annotated from API ID32E
74552Reimer, L.C., Lissin, A.,Schober, I., Witte,J.F., Podstawka, A., Lüken, H., Bunk, B.,Overmann, J.10.60712/SI-ID92372.1StrainInfo: A central database for resolving microbial strain identifiers
120969Curators of the CIPCollection of Institut Pasteur (CIP 104032)https://catalogue-crbip.pasteur.fr/fiche_catalogue.xhtml?crbip=CIP%20104032